FDA Recall
🇺🇸 United States
TerminatedTerminated: November 24, 2025Historical recordClass II
Lamb Weston Inc
- Product
- Item M7414, frozen foodservice Lamb Weston Hashbrown Patties…
- Reason
- Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Published
- May 14, 2025
- Distribution
- Distributed in Arizona and Hawaii and in…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: November 24, 2025Historical recordClass II
Lamb Weston Inc
- Product
- Item M0053, frozen foodservice Lamb Weston Hashbrown Patties…
- Reason
- Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Published
- May 14, 2025
- Distribution
- Distributed in Arizona and Hawaii and in…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: November 24, 2025Historical recordClass II
Lamb Weston Inc
- Product
- Item M7204, frozen foodservice Lamb Weston Hashbrown Patties…
- Reason
- Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Published
- May 14, 2025
- Distribution
- Distributed in Arizona and Hawaii and in…
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FDA Recall
OngoingHistorical recordClass II
Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, Manufactured for: Sandoz Inc., Princeton, NJ 08540, Distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product of Canada, NDC 54643-5649-1
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
- Published
- May 7, 2025
- Distribution
- Distributed to Medical Facilities in MS…
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FDA Recall
OngoingHistorical recordClass II
Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
- Published
- May 7, 2025
- Distribution
- Distributed to Medical Facilities in MS…
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FDA Recall
OngoingHistorical recordClass II
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC carton: 0517-0735-10 / NDC Vial: 0517-0735-01]
by American Regent, Inc.
- Reason
- Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, Mfd for: Civica, Inc., Lehi, UT 84043,Mfd by: American Regent, Inc., New Albany, OH 43064. NDC Carton: 72572-470-10/ NDC Vial: 72572-470-01.
by American Regent, Inc.
- Reason
- Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 90 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-452-15
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-450-17
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent
- Published
- May 7, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-448-17.
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent
- Published
- May 7, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-447-17
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent
- Published
- May 7, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles, Manufactured by: Glenmark Pharmaceuticals Limited, NDC 68788-8685-03.
by Preferred Pharmaceuticals, Inc.
- Reason
- cGMP Deviations
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL), 250 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-430-01
by Eugia US LLC
- Reason
- Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL), 100 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-429-01
by Eugia US LLC
- Reason
- Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
- Published
- May 7, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 5, 2025Historical recordClass II
Emily Kate's Foods
- Product
- Emily Kate's Gluten Free Carrot Cake, Net Wt. 6.4oz, Emily K…
- Reason
- Foreign material (foil) found in cake slices
- Published
- May 7, 2025
- Distribution
- One domestic consignee located in WI
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 5, 2025Historical recordClass II
Emily Kate's Foods
- Product
- Emily Kate's Gluten Free Vanilla Cake, Net Wt. 6.4oz, Emily…
- Reason
- Foreign material (foil) found in cake slices
- Published
- May 7, 2025
- Distribution
- One domestic consignee located in WI
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 1, 2026Historical recordClass II
MegaMex Foods LLC
- Product
- La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 7210…
- Reason
- Firm's salsa product was potentially manufactured with a recalled ingredient (Fresh Cilantro containing foreign objects "wood pieces")
- Published
- May 7, 2025
- Distribution
- Product was distributed to 9 consignees…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 1, 2025Historical recordClass II
Dinstuhl's Fine Candy Company, Inc.
- Product
- Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually…
- Reason
- Undeclared allergen (milk)
- Published
- May 7, 2025
- Distribution
- Three (3) retailers in MO and MS
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 1, 2025Historical recordClass II
Dinstuhl's Fine Candy Company, Inc.
- Product
- Dinstuhl's Peanut Brittle, NET WT 4 oz. (113g), individually…
- Reason
- Undeclared allergen (milk)
- Published
- May 7, 2025
- Distribution
- Three (3) retailers in MO and MS
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 1, 2025Historical recordClass II
Dinstuhl's Fine Candy Company, Inc.
- Product
- Dinstuhl's Cashew Crunch, NET WT 4 oz. (113g), individually…
- Reason
- Undeclared allergen (milk)
- Published
- May 7, 2025
- Distribution
- Three (3) retailers in MO and MS
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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